Hydrocarbon toxicity: Difference between revisions

 
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*Paint thinners
*Paint thinners
*Polish
*Polish
*[[Toluene]]
*Toluene


==Clinical Features==
==Clinical Features==
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==Differential Diagnosis==
==Differential Diagnosis==
{{Drugs of abuse types}}
{{Drugs of abuse types}}
*[[Chloral hydrate]]
 
{{Toxic gas exposure DDX}}


==Evaluation==
==Evaluation==
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===Pulmonary===
===Pulmonary===
*Secure airway, if needed.  
*Secure airway, if needed.  
*Beta2 agonist if wheezing (not proven benefit), consider [[Bipap]]/[[Cpap]] (may further barotrauma)
*Beta2 agonist if wheezing (not proven benefit), consider [[BiPAP]]/[[CPAP]] (may further barotrauma)
*Severe toxicity will need [[intubation]], high PEEP, possibly high frequency jet ventilation, and ECMO for refractory hypoxemia
*Severe toxicity will need [[intubation]], high PEEP, possibly high frequency jet ventilation, and ECMO for refractory hypoxemia
*Antibiotic prophylaxis show no benefit, but use if superinfection present
*Antibiotic prophylaxis show no benefit, but use if superinfection present
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===Cardiovascular===
===Cardiovascular===
*Treat hypotension with aggressive [[IVF]]
*Treat hypotension with aggressive [[IVF]]
*Avoid dopamine, epinephrine, norepinephrine (may cause dysrhythmias)
*Avoid [[dopamine]], [[epinephrine]], [[norepinephrine]] (may cause [[dysrhythmias]]), [[procainamide]] (may cause [[arrhythmias]]), and [[amiodarone]] ([[QT prolongation]])
*Treat ventricular dysrhythmias with [[propranolol]], [[esmolol]], or [[lidocaine]]
*Treat ventricular dysrhythmias with [[propranolol]], [[esmolol]], or [[lidocaine]]
**Due to overstimulation of beta receptors by hydrocarbon
**Due to overstimulation of beta receptors by hydrocarbon

Latest revision as of 20:58, 8 November 2023

Background

  • Typical exposures:
    • Unintentional exposure (generally young children)
    • Intentional abuse (generally adolescents, young adults)
    • Occupational exposure - dermal, inhalation
  • Intentional abuse methods:
    • Huffing= hydrocarbon soaked into rag and placed over mouth and nose
    • Bagging= hydrocarbon placed in a bag and fumes inhaled
    • Sniffing= hydrocarbon inhaled directly
  • High volatility, low viscosity → high risk for aspiration despite "simple ingestion"
  • Easily washes out pulmonary surfactant if aspirated

Examples

  • Gasoline
  • Lighter fluid
  • Lamp oil
  • Petroleum jelly (Vaseline)
  • Paint
  • Paint thinners
  • Polish
  • Toluene

Clinical Features

Pulmonary

  • Aspiration
    • Low viscosity and surface tension of hydrocarbons make them high aspiration risk
    • Additional risk factors: high volume, vomiting, gagging, choking, coughing
    • CXR on presentation nonpredictive, but usually appear by 6hrs
  • ARDS

Cardiac

  • Arrhythmias, Afib, PVCs, Vtach, torsades
  • "Sudden sniffing death syndrome"= suspected cardiac sensitization to catecholamines
    • Classic scenario: Sniffer is startled during use, collapses and dies

CNS/PNS [1]

Renal

  • Toluene in particular may cause weakness secondary to severe hypokalemia

Differential Diagnosis

Drugs of abuse

Toxic gas exposure

Evaluation

Workup

  • CXR: immediately if symptomatic, otherwise early CXR not predictive of pneumonitis. Observe for 4-6hrs then obtain CXR
  • Labs: as needed to evaluate for acidosis, anemia, renal/hepatic toxicity, coagulation, methemoglobinemia, carboxyhemoglobinemia depending on specific exposure
  • ECG

Evaluation

  • Clinical diagnosis, based on history and physical exam

Management

Pulmonary

  • Secure airway, if needed.
  • Beta2 agonist if wheezing (not proven benefit), consider BiPAP/CPAP (may further barotrauma)
  • Severe toxicity will need intubation, high PEEP, possibly high frequency jet ventilation, and ECMO for refractory hypoxemia
  • Antibiotic prophylaxis show no benefit, but use if superinfection present
  • Steroids not recommended for chemical pneumonitis and can lead to increased superinfection

Cardiovascular

Dermal

  • Pre-arrival decontamination, remove clothing
  • Soap and water, saline for eye exposure

GI

Disposition

Discharge

After 6 hour observation if:

  • Asymptomatic
  • Normal vital signs (including SpO2)
  • No abnormal pulmonary findings
  • Normal CXR at 6hrs post exposure
    • If asymptomatic but radiographic evidence of pneumonitis, consider discharge with 24-hour follow-up.

Admit

  • Clinical evidence of toxicity

See Also

References

  1. Tormoehlen L et al. Hydrocarbon toxicity: A review. Clinical toxicology 2014; 52: 479-489